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Crystal structure of apo-type bacterial vanadium-dependent chloroperoxidase

Analyse Crystal structure of apo-type bacterial vanadium-dependent chloroperoxidase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3W35
Type
protein
Length
922 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NAPH1
EC
1.11.1.10
UniProt
A7KH27
Pockets
8 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 49% helix, 8% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANAPH1 (EC 1.11.1.10)protein45950% helix, 8% strandA7KH27
BNAPH1 (EC 1.11.1.10)protein46348% helix, 7% strandA7KH27

Pockets

8 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18900.750.7977empty
24840.740.8239empty
38190.740.7867empty
46010.720.7953empty
5670.720.9825empty

Interfaces

1 interface between chains.

  • A–B · 2111 Ų buried · 30 hydrogen bonds · protein-protein

Compared structures

  • 3W35 · Crystal structure of apo-type bacterial Vanadium-dependent chloroperoxidase · the same entry in another collection · chain A against A, TM-score 1.00

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